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FDA 510(k)

GSA GENITO SENSORY ANALYZER

K-Number: K010981 · 2001-09-20

ApplicantMedoc Ltd. Advanced Medical Systems
Decision Date2001-09-20
Product CodeLLN
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

GSA GENITO SENSORY ANALYZER is the device name listed in this FDA 510(k) record. The listed applicant is Medoc Ltd. Advanced Medical Systems. It received FDA 510(k) clearance on 2001-09-20 under 510(k) number K010981. The device is classified under product code LLN. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GSA GENITO SENSORY ANALYZER?

GSA GENITO SENSORY ANALYZER is a medical device that received FDA 510(k) clearance on 2001-09-20. The listed applicant is Medoc Ltd. Advanced Medical Systems. The 510(k) number is K010981.

When did GSA GENITO SENSORY ANALYZER receive FDA 510(k) clearance?

GSA GENITO SENSORY ANALYZER received FDA 510(k) clearance on 2001-09-20, under 510(k) number K010981.

Who is the listed applicant for GSA GENITO SENSORY ANALYZER?

The FDA 510(k) record lists Medoc Ltd. Advanced Medical Systems as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for GSA GENITO SENSORY ANALYZER?

The FDA product code for GSA GENITO SENSORY ANALYZER is LLN.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Other records listing Medoc Ltd. Advanced Medical Systems as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K052357PATHWAY - ATS/CHEPSK051448MODIFIED CONTACT-HEAT EVOKED POTENTIAL STIMULATOR (CHEPS)K041908CONTACT HEAT-EVOKED POTENTIAL STIMULATOR (CHEPS)

Related Devices (Code: LLN)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K072882PAIN VISION, MODEL PS-2100Osachi Co., Ltd.K030829VPT METERXilas Medical, Inc.K964622MEDI-DX 7000Neuro-Diagnostic Assoc.K964815AP-4000, AIR PULSE SENSORY STIMULATORPentax Precision Instrument Corp.K970180VSA 3000 VIBRATORYN SENSORY ANALYZEREare Consulting ServiceK934368NK PRESSURE-SPECIFIED SENSORY DEVICE, MODEL PSSD-001Nk Biotechnical Engineering Co.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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